AIRLIFE? ARTERIAL BLOOD SAMPLER 9425TRU

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-31 for AIRLIFE? ARTERIAL BLOOD SAMPLER 9425TRU manufactured by Vyaire Medical.

MAUDE Entry Details

Report Number8030673-2019-00048
MDR Report Key8848360
Date Received2019-07-31
Date of Report2019-07-15
Date of Event2019-07-15
Date Mfgr Received2019-07-15
Date Added to Maude2019-07-31
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactSTANLEY TAN
Manufacturer Street22745 SAVI RANCH PKWY
Manufacturer CityYORBA LINDA CA 92887
Manufacturer CountryUS
Manufacturer Postal92887
Manufacturer Phone7149193324
Manufacturer G1PRODUCTOS UROLOGOS DE MEXICO S.A. DE C.V.
Manufacturer StreetCERRADA V #85 PARQUE UNDUSTRIAL
Manufacturer CityMEXICALI, 21397
Manufacturer CountryMX
Manufacturer Postal Code21397
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameAIRLIFE? ARTERIAL BLOOD SAMPLER
Generic NameARTERIAL BLOOD GAS PRODUCTS (ABG)
Product CodeCBT
Date Received2019-07-31
Catalog Number9425TRU
Lot Number0004084211
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerVYAIRE MEDICAL
Manufacturer Address22745 SAVI RANCH PKWY YORBA LINDA CA 92887 US 92887


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-07-31

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